Inducible HIV RNA transcription assays to measure HIV persistence: pros and cons of a compromise

Abstract With the increasing number of therapeutic strategies tested in humans to reduce the size of the latent reservoir, the development of a robust, precise and clinical trial scalable assay that measures the frequency of infected cells carrying inducible replication-competent HIV is urgently nee...

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Main Authors: Johann Plantin, Marta Massanella, Nicolas Chomont
Format: Article
Language:English
Published: BMC 2018-01-01
Series:Retrovirology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12977-017-0385-y
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spelling doaj-11e85c03356343109c99a54f18bc7bfc2020-11-24T21:54:40ZengBMCRetrovirology1742-46902018-01-0115111110.1186/s12977-017-0385-yInducible HIV RNA transcription assays to measure HIV persistence: pros and cons of a compromiseJohann Plantin0Marta Massanella1Nicolas Chomont2Department of Microbiology, Infectiology and Immunology, Faculté de Médecine, Université de MontréalDepartment of Microbiology, Infectiology and Immunology, Faculté de Médecine, Université de MontréalDepartment of Microbiology, Infectiology and Immunology, Faculté de Médecine, Université de MontréalAbstract With the increasing number of therapeutic strategies tested in humans to reduce the size of the latent reservoir, the development of a robust, precise and clinical trial scalable assay that measures the frequency of infected cells carrying inducible replication-competent HIV is urgently needed. The size of the pool of cells carrying replication-competent HIV is largely overestimated by DNA assays, as a result of a large proportion of defective viruses, and underestimated by co-culture outgrowth assays. New culture methods that measure the inducible HIV reservoir have been developed during the past few years. In these induction assays, CD4+ T cells from virally suppressed individuals are activated and HIV RNA is measured in cell extracts or cell supernatants. In this review, we summarize the principle and outcomes of these assays and discuss the potential of these methods in the evaluation of HIV eradication strategies.http://link.springer.com/article/10.1186/s12977-017-0385-yHIV reservoirInduced RNAHIV transcription
collection DOAJ
language English
format Article
sources DOAJ
author Johann Plantin
Marta Massanella
Nicolas Chomont
spellingShingle Johann Plantin
Marta Massanella
Nicolas Chomont
Inducible HIV RNA transcription assays to measure HIV persistence: pros and cons of a compromise
Retrovirology
HIV reservoir
Induced RNA
HIV transcription
author_facet Johann Plantin
Marta Massanella
Nicolas Chomont
author_sort Johann Plantin
title Inducible HIV RNA transcription assays to measure HIV persistence: pros and cons of a compromise
title_short Inducible HIV RNA transcription assays to measure HIV persistence: pros and cons of a compromise
title_full Inducible HIV RNA transcription assays to measure HIV persistence: pros and cons of a compromise
title_fullStr Inducible HIV RNA transcription assays to measure HIV persistence: pros and cons of a compromise
title_full_unstemmed Inducible HIV RNA transcription assays to measure HIV persistence: pros and cons of a compromise
title_sort inducible hiv rna transcription assays to measure hiv persistence: pros and cons of a compromise
publisher BMC
series Retrovirology
issn 1742-4690
publishDate 2018-01-01
description Abstract With the increasing number of therapeutic strategies tested in humans to reduce the size of the latent reservoir, the development of a robust, precise and clinical trial scalable assay that measures the frequency of infected cells carrying inducible replication-competent HIV is urgently needed. The size of the pool of cells carrying replication-competent HIV is largely overestimated by DNA assays, as a result of a large proportion of defective viruses, and underestimated by co-culture outgrowth assays. New culture methods that measure the inducible HIV reservoir have been developed during the past few years. In these induction assays, CD4+ T cells from virally suppressed individuals are activated and HIV RNA is measured in cell extracts or cell supernatants. In this review, we summarize the principle and outcomes of these assays and discuss the potential of these methods in the evaluation of HIV eradication strategies.
topic HIV reservoir
Induced RNA
HIV transcription
url http://link.springer.com/article/10.1186/s12977-017-0385-y
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